Age-associated distribution of normal B-cell and plasma cell subsets in peripheral blood
Autor: | Blanco, E., Perez-Andres, M., Arriba-Mendez, S., Contreras-Sanfeliciano, T., Criado, I., Pelak, O., Serra-Caetano, A., Romero, A., Puig, N., Remesal, A., Canizales, J.T., Lopez-Granados, E., Kalina, T., Sousa, A.E., Zelm, M. van, Burg, M. van der, Dongen, J.J.M. van, Orfao, A., EuroFlow PID Grp |
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Přispěvatelé: | Repositório da Universidade de Lisboa, Immunology, Ministerio de Economía y Competitividad (España), Ministry of Education, Youth and Sports (Czech Republic), Junta de Castilla y León, Instituto de Salud Carlos III, European Commission |
Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Adult Male Normal B cells Aging Adolescent Immunology Plasma Cells Immunoglobulins Reference ranges chemical and pharmacologic phenomena Plasma cell Biology Immunoglobulin D 03 medical and health sciences Young Adult medicine Immunology and Allergy Humans Age-related values Flow cytometry IgH isotype Child B cell Aged Aged 80 and over B-Lymphocytes Infant Newborn Infant Middle Aged Memory B cells Isotype Subclass Immunoglobulin Class Switching Immunity Humoral Immunoglobulin Isotypes 030104 developmental biology medicine.anatomical_structure Immunoglobulin class switching Child Preschool biology.protein Immunoglobulin heavy chain Female Antibody Immunoglobulin Heavy Chains Nephelometry Immunologic Memory |
Zdroj: | Journal of Allergy and Clinical Immunology, 141(6), 2208 Journal of Allergy and Clinical Immunology, 141(6), 2208-+. Mosby Inc. Digital.CSIC. Repositorio Institucional del CSIC instname |
ISSN: | 1097-6825 0091-6749 |
Popis: | On behalf of the EuroFlow PID group. [Background]: Humoral immunocompetence develops stepwise throughout life and contributes to individual susceptibility to infection, immunodeficiency, autoimmunity, and neoplasia. Immunoglobulin heavy chain (IgH) isotype serum levels can partly explain such age-related differences, but their relationship with the IgH isotype distribution within memory B-cell (MBC) and plasma cell (PCs) compartments remains to be investigated. [Objective]: We studied the age-related distribution of MBCs and PCs expressing different IgH isotypes in addition to the immature/transitional and naive B-cell compartments. [Methods]: B-cell and PC subsets and plasma IgH isotype levels were studied in cord blood (n = 19) and peripheral blood (n = 215) from healthy donors aged 0 to 90 years by using flow cytometry and nephelometry, respectively. [Results]: IgH-switched MBCs expressing IgG, IgG, IgG, IgA, and IgA were already detected in cord blood and newborns at very low counts, whereas CD27IgMIgD MBCs only became detectable at 1 to 5 months and remained stable until 2 to 4 years, and IgD MBCs peaked at 2 to 4 years, with both populations decreasing thereafter. MBCs expressing IgH isotypes of the second immunoglobulin heavy chain constant region (IGHC) gene block (IgG, IgG, and IgA) peaked later during childhood (2-4 years), whereas MBCs expressing third IGHC gene block immunoglobulin isotypes (IgG, IgG, and IgA) reached maximum values during adulthood. PCs were already detected in newborns, increasing in number until 6 to 11 months for IgM, IgG, IgG, IgG, IgA, and IgA; until 2 to 4 years for IgD; and until 5 to 9 years for IgG and decreasing thereafter. For most IgH isotypes (except IgD and IgG), maximum plasma levels were reached after PC and MBC counts peaked. [Conclusions]: PC counts reach maximum values early in life, followed by MBC counts and plasma IgH isotypes. Importantly, IgH isotypes from different IGHC gene blocks show different patterns, probably reflecting consecutive cycles of IgH isotype switch recombination through life. E.B. was supported by a grant from Junta de Castilla y León (Fondo Social Europeo, ORDEN EDU/346/2013, Valladolid, Spain). This work was supported by the CB16/ 12/00400 grant (CIBERONC, Instituto de Salud Carlos III, Ministerio de Economía y Competitividad, Madrid, Spain, and FONDOS FEDER) and the FIS PI12/00905-FEDER grant from the Fondo de Investigaciones Sanitarias of Instituto de Salud Carlos III (Madrid, Spain). O.P. and T.K. were supported by the Ministry of Education, Youth and Sports (NPU I no. LO1604 and 15-28541A). The coordination and innovation processes of this study were supported by the EuroFlow Consortium. |
Databáze: | OpenAIRE |
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